Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906608
rs387906608
A 0.810 CausalMutation CLINVAR

dbSNP: rs267606746
rs267606746
A 0.800 CausalMutation CLINVAR

dbSNP: rs112638391
rs112638391
0.700 GeneticVariation UNIPROT

dbSNP: rs113828929
rs113828929
A 0.700 CausalMutation CLINVAR

dbSNP: rs121434554
rs121434554
A 0.700 CausalMutation CLINVAR

dbSNP: rs121912937
rs121912937
G 0.700 CausalMutation CLINVAR

dbSNP: rs1255514828
rs1255514828
0.700 GeneticVariation UNIPROT

dbSNP: rs137964147
rs137964147
T 0.700 GeneticVariation CLINVAR

dbSNP: rs150168522
rs150168522
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1568931397
rs1568931397
G 0.700 CausalMutation CLINVAR

dbSNP: rs1569518138
rs1569518138
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1569518677
rs1569518677
T 0.700 GeneticVariation CLINVAR

dbSNP: rs267606747
rs267606747
C 0.700 CausalMutation CLINVAR

dbSNP: rs267606748
rs267606748
0.700 GeneticVariation UNIPROT

dbSNP: rs267606749
rs267606749
0.700 GeneticVariation UNIPROT

dbSNP: rs398122821
rs398122821
T 0.700 CausalMutation CLINVAR

dbSNP: rs398124119
rs398124119
A 0.700 CausalMutation CLINVAR

dbSNP: rs748035948
rs748035948
T 0.700 CausalMutation CLINVAR

dbSNP: rs764193290
rs764193290
C 0.700 GeneticVariation CLINVAR

dbSNP: rs771941724
rs771941724
A 0.700 GeneticVariation CLINVAR

dbSNP: rs797044457
rs797044457
T 0.700 CausalMutation CLINVAR

dbSNP: rs797044458
rs797044458
T 0.700 CausalMutation CLINVAR

dbSNP: rs797044988
rs797044988
G 0.700 GeneticVariation CLINVAR

dbSNP: rs886039905
rs886039905
GT 0.700 GeneticVariation CLINVAR

dbSNP: rs387906608
rs387906608
0.810 GeneticVariation UNIPROT Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy. 15689448

2005